Canonical Allele Identifier: CA2015109434

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604522_8604524delinsAAG , CM000674.2:g.8604522_8604524delinsAAG	GRCh38
NC_000012.11:g.8757118_8757120delinsAAG , CM000674.1:g.8757118_8757120delinsAAG	GRCh37
NC_000012.10:g.8648385_8648387delinsAAG	NCBI36
NG_011588.1:g.13323_13325delinsCTT , LRG_17:g.13323_13325delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.514-187_514-185delinsCTT	ENSP00000445691.1:n.514-187_514-185delinsCTT
ENST00000543081.6:c.428-187_428-185delinsCTT	ENSP00000439103.2:n.428-187_428-185delinsCTT
ENST00000544516.6:c.157-187_157-185delinsCTT	ENSP00000439538.2:n.157-187_157-185delinsCTT
ENST00000545576.2:n.945-187_945-185delinsCTT
ENST00000696246.1:c.499-187_499-185delinsCTT	ENSP00000512504.1:n.499-187_499-185delinsCTT
ENST00000696271.1:n.956-187_956-185delinsCTT
ENST00000696272.1:c.529-187_529-185delinsCTT	ENSP00000512515.1:n.529-187_529-185delinsCTT
ENST00000696273.1:c.577-187_577-185delinsCTT	ENSP00000512516.1:n.577-187_577-185delinsCTT
ENST00000229335.11:c.544-187_544-185delinsCTT MANE Select	ENSP00000229335.6:n.544-187_544-185delinsCTT
ENST00000229335.10:c.544-187_544-185delinsCTT	ENSP00000229335.6:n.544-187_544-185delinsCTT
ENST00000537228.5:c.514-187_514-185delinsCTT	ENSP00000445691.1:n.514-187_514-185delinsCTT
ENST00000543081.5:c.424-187_424-185delinsCTT
ENST00000544516.5:c.153-187_153-185delinsCTT
ENST00000545512.1:c.540-187_540-185delinsCTT
ENST00000545576.1:n.870-187_870-185delinsCTT
NM_020661.2:c.544-187_544-185delinsCTT , LRG_17t1:c.544-187_544-185delinsCTT	NP_065712.1:n.544-187_544-185delinsCTT
XM_011520772.1:c.514-187_514-185delinsCTT	XP_011519074.1:n.514-187_514-185delinsCTT
XM_011520773.1:c.428-187_428-185delinsCTT	XP_011519075.1:n.428-187_428-185delinsCTT
NM_001330343.1:c.514-187_514-185delinsCTT	NP_001317272.1:n.514-187_514-185delinsCTT
NM_020661.3:c.544-187_544-185delinsCTT	NP_065712.1:n.544-187_544-185delinsCTT
XM_011520773.2:c.428-187_428-185delinsCTT	XP_011519075.1:n.428-187_428-185delinsCTT
NM_020661.4:c.544-187_544-185delinsCTT MANE Select	NP_065712.1:n.544-187_544-185delinsCTT
NM_001330343.2:c.514-187_514-185delinsCTT	NP_001317272.1:n.514-187_514-185delinsCTT